Contract · No Set aside used
TECHNOLOGY LICENSING OPPORTUNITY: NanoFET
- Agency
- ENERGY, DEPARTMENT OF / ENERGY, DEPARTMENT OF
- Location
- Los Alamos, NM
- Amount
- Amount not listed
- Deadline
- Closes in 152 days (Dec 17, 2026)
- Posted
- Jun 17, 2026
- Set-aside
- No Set aside used
- NAICS code
- 541714
What this contract is for
NanoFiber Engineered Therapeutics Platform (NanoFET) from Los Alamos National Laboratory offers pharmaceutical and biodefense organizations a modular, adaptable scaffold for building next-generation immunotherapies. By merging self-assembling peptide nanofibers with interchangeable nanobody and peptide components, the platform enables rapid development of targeted treatments that bridge disease agents directly to the patient’s own immune cells. Infectious diseases and chronic conditions such as cancer continue to impose enormous public health and economic burdens worldwide. Conventional vaccines and biologics are typically designed against a single pathogen or target, leaving populations vulnerable when new or unknown threats emerge. For military personnel and first responders, the absence of broad-spectrum medical countermeasures means that exposure to an unidentified pathogen in the field can be met with little more than supportive care. In cancer immunotherapy, connecting tumor cells to the patient’s own immune effector cells remains a formidable engineering challenge; current bispecific antibody formats are complex to manufacture, expensive and often limited in the number of targets they can engage simultaneously. Meanwhile, traditional antibody-based therapeutics are large molecules that can be difficult to produce at scale, may trigger unwanted immune reactions and lack the modularity needed for rapid adaptation to new disease targets. A platform capable of addressing multiple threats through a single reconfigurable architecture would represent a meaningful shift in how therapeutics are developed and deployed. Advantages: Modular architecture allows rapid swapping of nanobodies and peptides to address new disease targets without redesigning the core platform Dual-...
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